Canonical Allele Identifier: CA1041263305

Gene: TMEM237

Linked Data

• dbSNP Id: rs1957758727
• gnomAD v3: 2-201626333-G-A
• gnomAD v4: 2-201626333-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626333G>A , CM000664.2:g.201626333G>A	GRCh38
NC_000002.11:g.202491056G>A , CM000664.1:g.202491056G>A	GRCh37
NC_000002.10:g.202199301G>A	NCBI36
NG_032049.1:g.22197C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-186C>T
ENST00000621467.5:c.912-186C>T	ENSP00000480508.2:n.912-186C>T
ENST00000686475.1:n.978-186C>T
ENST00000409883.7:c.1038-186C>T MANE Select	ENSP00000386264.2:n.1038-186C>T
ENST00000286196.9:c.*602-186C>T	ENSP00000286196.5:n.*602-186C>T
ENST00000409444.6:c.1014-186C>T	ENSP00000387203.2:n.1014-186C>T
ENST00000409883.6:c.1038-186C>T	ENSP00000386264.2:n.1038-186C>T
ENST00000471318.5:n.266-186C>T
ENST00000621467.4:c.1014-186C>T	ENSP00000480508.1:n.1014-186C>T
NM_001044385.2:c.1038-186C>T	NP_001037850.1:n.1038-186C>T
NM_152388.3:c.1014-186C>T	NP_689601.2:n.1014-186C>T
NM_001044385.3:c.1038-186C>T MANE Select	NP_001037850.1:n.1038-186C>T
NM_152388.4:c.1014-186C>T	NP_689601.2:n.1014-186C>T